New Episodes Every Wednesday

Episodes

234: Expert Child Life Tips for Supporting Children Through an Upper GI Procedure
Nov. 12, 2024

234: Expert Child Life Tips for Supporting Children Through an Upper …

Today's episode is dedicated to the loving memory of Dr. Meredith Hitch, a cherished pediatric gastroenterologist at Ochsner Baton Rouge. "You want to make sure that you are ready to be able to prepare not only yourself but y...

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233: From NICU Nurse to NICU Mom: Premature Twins born at 33 weeks - Brittney's Story
Oct. 29, 2024

233: From NICU Nurse to NICU Mom: Premature Twins born at 33 weeks - …

A huge thank you to our sponsor of today's podcast, Begin Health. - Use code CHILDLIFEONCALL for 25% off 30% of children struggle with constipation and it can feel impossible trying to find a solution for your child. Especia...

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232: Preparing and Supporting your child: A son with Breath Holding Spells-Alessandra's Story
Oct. 15, 2024

232: Preparing and Supporting your child: A son with Breath Holding S…

A huge thank you to our sponsor of today's podcast, Begin Health. - Use code CHILDLIFEONCALL for 25% off 30% of children struggle with constipation and it can feel impossible trying to find a solution for your child. Especia...

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231: Child Life Specialist Secrets: Flu Shot Prep Strategies Every Parent Should Know
Oct. 6, 2024

231: Child Life Specialist Secrets: Flu Shot Prep Strategies Every Pa…

Child Life Specialist Secrets: Flu Shot Prep Strategies Every Parent Should Know Thank you to the sponsor of today's podcast: Begin Health In this episode of the Child Life On Call Podcast, hosts Katie Taylor and Emily Martin...

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230: Navigating Childhood Cancer: Supporting families through her own experience - Heather's Story
Sept. 24, 2024

230: Navigating Childhood Cancer: Supporting families through her own…

230: Navigating Childhood Cancer: Supporting families through her own experience - Heather's Story "We've joined a club that nobody wants to be a part of, but the good part is we have the best members." A huge thank you to ou...

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229: Trusting your parental Instincts when addressing your child's chronic pain- A son with Juvenile Arthritis- Kim's Story
Sept. 17, 2024

229: Trusting your parental Instincts when addressing your child's ch…

"Trust your gut. If your parent radar comes up and says this is not right, keep pushing." – Kim In this episode, Katie Taylor speaks with Kim Miller, a mother whose journey navigating her son Grant's diagnoses of juvenile art...

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228: Early Diagnosis, Advocacy and Equity: A daughter with Cystic Fibrosis- Nikki's Story
Sept. 3, 2024

228: Early Diagnosis, Advocacy and Equity: A daughter with Cystic Fib…

"We are the experts on our daughter and we deserve a say, and we deserve to be given the time to ask questions." – Nikki DeLeo We extend our sincere gratitude to our sponsor for this episode, Gebauer PainEase®. We are pleased...

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227: Searching for a Diagnosis: A Rare Disease Mom and Advocate's Journey - ADCY5 Gay's Story
Aug. 20, 2024

227: Searching for a Diagnosis: A Rare Disease Mom and Advocate's Jou…

"If you have a doubt about something with your child or a family member, it's just really important to keep pushing through and get to the answers." – Gay Grossman In this episode, host Katie Taylor speaks with Gay Grossman, ...

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226. Moms on a Mission: Raising Pediatric Feeding Disorder Awareness with Jaclyn & Athena from Feeding Matters
Aug. 6, 2024

226. Moms on a Mission: Raising Pediatric Feeding Disorder Awareness …

"Combining my personal experiences as a mom with my professional role has given me a unique perspective on the challenges families face and the solutions they need." - Jaclyn Pederson In this insightful episode, host Katie Ta...

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225: Embracing Alopecia: A Mother's Journey of Advocacy, Instincts, and Resilience-Lexi's Story
July 23, 2024

225: Embracing Alopecia: A Mother's Journey of Advocacy, Instincts, a…

"I feel like I owe it to him to explore other avenues. Acceptance doesn't mean giving up; it means continuing to learn and adapt."- Lexi In this episode of Child Life On Call, Katie Taylor speaks with Lexi, a devoted mother o...

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224: A son with Burkitt lymphoma at 8 year's old - Reina's Story
July 9, 2024

224: A son with Burkitt lymphoma at 8 year's old - Reina's Story

"My immediate thought was I'm going to lose my son. That was where my head went immediately." - Reina Introduction In this episode of Child Life On Call, Katie Taylor talks with Reina, a devoted mother from Nashville, Tenness...

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223: [6 minutes] Big News: The Child Life On Call App is Now SupportSpot!
June 30, 2024

223: [6 minutes] Big News: The Child Life On Call App is Now SupportS…

Episode Description: In this special impromptu episode, Katie Taylor, Certified Child Life Specialist and CEO of Child Life On Call, shares some exciting news! We're rebranding our beloved Child Life On Call app to SupportSpo...

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222: A son born at 25 weeks after loss, NICU NP mom and podcaster: Ashley O'Neil
June 25, 2024

222: A son born at 25 weeks after loss, NICU NP mom and podcaster: As…

In this episode host Katie Taylor sits down with Ashley O'Neil, a family nurse practitioner and a NICU mom. Ashley shares her journey when her son, Colin, was born at 25 weeks gestation and the following 183 day NICU stay. L...

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221:Collaborative care between a Child Life Specialist and Social Worker with Annie Gunning and Haley Thomas at Hope for HIE
June 11, 2024

221:Collaborative care between a Child Life Specialist and Social Wor…

On today's episode, Katie had the privilege of speaking with Annie Gunning , a Certified Child Life Specialist and Grief Counselor, and Haley Thomas , a Licensed Master Social Worker, on their collaborative efforts to support...

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220: Know EXACTLY When Rounds is Happening with Q-Rounds with Dr. Michael Pitt
May 28, 2024

220: Know EXACTLY When Rounds is Happening with Q-Rounds with Dr. Mic…

Episode Description: Join Katie Taylor, CCLS in this episode as she talks with Dr. Michael Pitt the founder of Q-Rounds and a compassionate pediatrician (and magician!) dedicated to enhancing doctor-patient communication. As ...

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219: 60 Years Later: Reflecting on a Daughter with Ichthyosis
May 21, 2024

219: 60 Years Later: Reflecting on a Daughter with Ichthyosis

"We, we weren't letting those people push us around because, believe it or not, living with us 24 hours a day, we knew more than some of the doctors." - Skip Vilas In this heartfelt episode of the Child Life On Call podcast, ...

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218: How NOT to Give Families Medical Information - A son with CHARGE syndrome, Taylor's Story
May 14, 2024

218: How NOT to Give Families Medical Information - A son with CHARGE…

Today's guest is Taylor Happley, a mom of a child with CHARGE syndrome. "We need to figure out why and how to help these kids get the medical attention that they need." In today's episode, Katie Taylor had an important conver...

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217: Navigating IEPs, Infantile Spasms, NICU & STXBP1 - Erin's Story
May 7, 2024

217: Navigating IEPs, Infantile Spasms, NICU & STXBP1 - Erin's Story

Today's guest is Erin Prosser, an IEP expert consultant and a mom of a daughter diagnosed with STXBP1. "You don't see it coming. Being a rare disease parent hits you like a ton of bricks." In today's episode Katie Taylor had ...

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216: How to talk with Kids about Child Abuse - Jane's Story [Repost]
April 23, 2024

216: How to talk with Kids about Child Abuse - Jane's Story [Repost]

April is Child Abuse Prevention Awareness Month. We have reposted this episode to bring awareness and give you tangible tools to speak with your kids about child abuse. Today's guest expert is Jane Donovan, who is a child abu...

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215: Ruptured Appendix: Emergent Surgery, 6 Days in the Hospital & Struggles to Discharge - Aspen's Story
April 16, 2024

215: Ruptured Appendix: Emergent Surgery, 6 Days in the Hospital & St…

"I've learned so much in this whole process. It's like you have a depth inside of you that resurrects as an advocate and high alert, and it lives inside of you when you need it." -Aspen, Willa's Mom In this episode of Child L...

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214: Sacrifice, Advocacy, Joy: Raising a Son with End Stage Kidney Disease - The Ransome Family's Story
April 9, 2024

214: Sacrifice, Advocacy, Joy: Raising a Son with End Stage Kidney Di…

"Sometimes it's really therapeutic though to remember all that you have gone through because I feel like there are times when we look at each other and I'm like how did we get here?" -Tayler Ransome We're grateful for our spo...

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213: Parents, CCLS, Students: Show Up Exactly As You Are
April 2, 2024

213: Parents, CCLS, Students: Show Up Exactly As You Are

In This Episode: Katie Taylor goes off the beaten path in this special episode to share a profound moment of inspiration that struck her. This episode is a heartfelt message to child life specialists, students, and parents, e...

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212: CCLS Story: 18 Years of Supporting Kidney Families -Julie's Story
March 26, 2024

212: CCLS Story: 18 Years of Supporting Kidney Families -Julie's Story

"As a child life specialist, watching my tiniest patients grow and accomplish so many things is my favorite part of the job." - Julie, Certified Child Life Specialist Episode Summary: In this heartfelt episode of Child Life O...

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211: A Son Born with End-Stage Kidney Disease (Part 1): Lyndsey's Story
March 19, 2024

211: A Son Born with End-Stage Kidney Disease (Part 1): Lyndsey's Sto…

"Having a medically complex child, it's like everything's fine. And then, you know, we have a morning where we've thrown up a lot or our blood pressure is too low, and it just doesn't look good. You just never know what you'r...

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